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Philippines FDA registration MDR-01442

SUPER TORQUE ® PLUS Diagnostic Catheter

PhilippinesCordis US Corp.- 14201 North West 60th Avenue, Miami Lakes, Florida, 33014 USA mfd by: Cardinal Health Mexico 244 S.de R.L.de C.V- Santiago Troncoso 808 Parque Industrial Salvacar Ciudad Juarez Chihuahua CP 32574 MexicoMexicoIssued March 10, 2025 – August 14, 2029
VerifiedFDA Philippines · official registry
Device information
Product Name
SUPER TORQUE ® PLUS Diagnostic Catheter
Registration Number
MDR-01442
Manufacturer details
Manufacturer
Cordis US Corp.- 14201 North West 60th Avenue, Miami Lakes, Florida, 33014 USA mfd by: Cardinal Health Mexico 244 S.de R.L.de C.V- Santiago Troncoso 808 Parque Industrial Salvacar Ciudad Juarez Chihuahua CP 32574 Mexico
Country of Origin
Mexico
Importer & distribution
Importer/Distributor
Getz Bros. Philippines, Inc.
Registration dates
Issuance Date
March 10, 2025
Expiry Date
August 14, 2029
About this record

Access comprehensive regulatory information for SUPER TORQUE ® PLUS Diagnostic Catheter in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01442 and manufactured by Cordis US Corp.- 14201 North West 60th Avenue, Miami Lakes, Florida, 33014 USA mfd by: Cardinal Health Mexico 244 S.de R.L.de C.V- Santiago Troncoso 808 Parque Industrial Salvacar Ciudad Juarez Chihuahua CP 32574 Mexico in Mexico. The device was registered on March 10, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Getz Bros. Philippines, Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.